MS 275
Chemical Name: (Pyridin-3-yl)methyl 4-(2-aminophenylcarbamoyl)benzylcarbamate
Purity: ≥99%
Biological Activity
MS 275 is a class I HDAC inhibitor (IC50 values are 0.18, 0.74, 44.9 and >100 μM for HDAC1, 3, 8 and 6, respectively). Exhibits antiproliferative effects and induces apoptosis in a range of tumor cell lines in vitro and in vivo. Increases estrogen receptor α- and aromatase expression in breast cancer cells. Inhibits PCB-induced neuronal cell death by preventing HDAC3 binding and histone deacetylation within the synapsin-1 promoter.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors.
Saito et al.
Proc.Natl.Acad.Sci., 1999;96:4592 -
Distinct pharmacological properties of second generation HDAC inhibitors with the benzamide or hydroxamate head group.
Beckers et al.
Int.J.Cancer, 2007;121:1138 -
MS-275 inhibits aroclor 1254-induced SH-SY5Y neuronal cell toxicity by preventing the formation of the HDAC3/REST complex on the synapsin-1 promoter.
Formisano et al.
J.Pharmacol.Exp.Ther., 2015;352:236 -
Functional activation of the estrogen receptor-α and aromatase by the HDAC inhibitor entinostat sensitizes ER-negative tumors to letr.
Sabnis et al.
Cancer Res., 2011;71:1893
Product Datasheets
Citations for MS 275
The citations listed below are publications that use Tocris products. Selected citations for MS 275 include:
2 Citations: Showing 1 - 2
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Differential effects of HDAC inhibitors on PPN oscillatory activity in vivo.
Authors: Verónica Et al.
Neuropharmacology 2020;165:107922
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Suppression of TGFβ-mediated conversion of endothelial cells and fibroblasts into cancer associated (myo)fibroblasts via HDAC inhibition.
Authors: Kim
Br J?Cancer 2018;118(10):1359
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